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. 2005 Aug 16;106(13):4269–4277. doi: 10.1182/blood-2005-04-1679

Figure 2.

Figure 2.

MN1-TEL–expressing mice develop altered myelopoiesis de novo. (A) Increased GFP+ cells in BM of MN1-TEL–expressing mice, which died of severe anemia without T-lymphoid tumor (anemic cases). Numbers indicated are mean ± SE percentage of GFP+ cells (n = 3). MT/Cre indicates control MN1-TEL/Mx1-Cre BM cells 1 month (1 mo.) or 8 months (8 mo.) after treatment with pI-pC. (B) Increased Mac1+Gr1- cells in MN1-TEL–expressing mice. The entire population of BM cells was analyzed by FCM. (Left) Age-matched control MN1-TEL/Mx1-Cre BM cells not induced with pI-pC. (Right) BM cells of MN1-TEL–expressing mice with increased number of GFP+ cells. Numbers indicated are mean ± SE percentage (n = 3). (C) Mac1+/Gr1- cells in GFP+ or GFP- BM cells of MN1-TEL–expressing mice with increased number of GFP+ cells. Gates were set to select the 10% GFP-brightest or -dimmest population in MN1-TEL–expressing mice to clearly discriminate MN1-TEL+ and MN1-TEL- cells. Numbers indicated are mean ± SE percentage (n = 3). (Top) Mac1/Gr1 expression in GFP+ or GFP- BM cells. (Bottom) FSC and SSC of Mac1+/Gr1- cells in GFP+ or GFP- BM cells.